Global Variome shared LOVD

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Phenotype #0000021117 Individual ID 00024997 Associated disease HRFTC Phenotype details see paper; all members abnormally elevated serum ferritin levels, bilateral cataract (except V4 14y only single fleck one lens) Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2014-11-30 16:14:07 +01:00 (CET) Date last edited 2014-11-30 16:18:05 +01:00 (CET)

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